Patient

Patient

C.7.1.1

M

Clinical Trial Subject

C.7.1.3

U

Study

General Study

C.7.2.1

M

Patient Study

C.7.2.2

U

Clinical Trial Study

C.7.2.3

U

Series

General Series

C.7.3.1

M

Clinical Trial Series

C.7.3.2

U

DX Series

C.8.11.1

M

Mammography Series

C.8.11.6

M

Frame of Reference

Frame of Reference

C.7.4.1

C - Required if multiple images are obtained without releasing breast compression

Equipment

General Equipment

C.7.5.1

M

Image

General Image

C.7.6.1

M

Image Pixel

C.7.6.3

M

Contrast/Bolus

C.7.6.4

U

Display Shutter

C.7.6.11

U

Device

C.7.6.12

U

Intervention

C.7.6.13

U

Specimen

C.7.6.22

U

DX Anatomy Imaged

C.8.11.2

M

DX Image

C.8.11.3

M

DX Detector

C.8.11.4

M

X-Ray Collimator

C.8.7.3

U

DX Positioning

C.8.11.5

U

X-Ray Tomography Acquisition

C.8.7.7

U

X-Ray Acquisition Dose

C.8.7.8

U

X-Ray Generation

C.8.7.9

U

X-Ray Filtration

C.8.7.10

U

X-Ray Grid

C.8.7.11

U

Mammography Image

C.8.11.7

M

Overlay Plane

C.9.2

C - Required if graphic annotation is present - See Section A.27.3

VOI LUT

C.11.2

C - Required if Presentation Intent Type (0008,0068) is FOR PRESENTATION. Shall not be present otherwise.

Image Histogram

C.11.5

U

Acquisition Context

C.7.6.14

M

SOP Common

C.12.1

M

Common Instance Reference

C.12.2

U